Daniella Helena Hock

7PUBLICATIONS
48CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Medical devicesGene and molecular therapyMedical biochemistry - inorganic elements and compoundsMedical infection agents (incl. prions)
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Publications (7)

|Mar 31, 2025
Review: Utility of mass spectrometry in rare disease research and diagnosis.

Teresa Zhao, Daniella H Hock, James Pitt

|Feb 23, 2023
TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease.

Lindsey Van Haute, Emily O'Connor, Héctor Díaz-Maldonado

|Jan 29, 2022
Oligonucleotide correction of an intronic TIMMDC1 variant in cells of patients with severe neurodegenerative disorder.

Raman Kumar, Mark A Corbett, Nicholas J C Smith

|Jan 21, 2022
Biallelic Variants in PYROXD2 Cause a Severe Infantile Metabolic Disorder Affecting Mitochondrial Function.

Nicole J Van Bergen, Daniella H Hock, Lucy Spencer

|Apr 21, 2021
Optic atrophy-associated TMEM126A is an assembly factor for the ND4-module of mitochondrial complex I.

Luke E Formosa, Boris Reljic, Alice J Sharpe

|Apr 10, 2021
Coding and non-coding roles of MOCCI (C15ORF48) coordinate to regulate host inflammation and immunity.

Cheryl Q E Lee, Baptiste Kerouanton, Sonia Chothani

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Frequent Collaborators

7 joint publications

David Arthur Stroud

4 joint publications

John Christodoulou

4 joint publications

David R Thorburn

2 joint publications

Guy Helman